Diseases |
Alias |
|
Pelizaeus-Merzbacher Disease |
PMD
|
HLD1
|
Pelizaeus-Merzbacher Brain Sclerosis
|
Leukodystrophy, Hypomyelinating, 1
|
Diffuse Familial Brain Sclerosis
|
Pelizaeus Merzbacher Brain Sclerosis
|
Sudanophilic Leukodystrophy, Paelizeus-Merzbacher Type
|
Cockayne-Pelizaeus-Merzbacher Disease
|
Hypomyelinating Leukodystrophy 1
|
Leukodystrophy, Sudanophilic
|
Pelizaeus Merzbacher Disease
|
Hypomyelinating Leukodystrophy, 1
|
Sudanophilic Leukodystrophy
|
Pelizaeus-Merzbacher Disease, Connatal Form
|
Connatal Pmd
|
Pelizaeus-Merzbacher Disease Type Ii
|
Severe Pmd
|
Null Syndrome
|
Plp1 Null Syndrome
|
Pelizaeus-Merzbacher Disease, Null Syndrome
|
Brain Sclerosis Diffuse Familial
|
Sudanophilic Leukodystrophy Paelizeus-Merzbacher Type
|
Leukodystrophy Hypomyelinating 1
|
Diffuse Cerebral Sclerosis Of Schilder
|
|
|
Spastic Paraplegia 2, X-Linked |
SPG2
|
Hereditary Spastic Paraplegia 2
|
Sppx2
|
Spastic Paraplegia Type 2
|
Spastic Paraplegia 2
|
Hereditary X-Linked Recessive Spastic Paraplegia
|
X-Linked Spastic Paraplegia 2
|
X Linked Recessive Hereditary Spastic Paraplegia
|
Spastic Gait Type 2
|
Spastic Paraparesis Type 2
|
X-Linked Spastic Paraplegia Type 2
|
Spastic Paraplegia Type 2, X-Linked
|
Spastic Paraplegia-2
|
Paraplegia, Spastic, Type 2
|
|
|
Pelizaeus-Merzbacher Disease, Classic Form |
|
|
Pelizaeus-Merzbacher Disease, Transitional Form |
|
|
Pelizaeus-Merzbacher Disease In Female Carriers |
|
|
Hypomyelination Of Early Myelinating Structures |
|
|
Hereditary Spastic Paraplegia |
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
Hsp
|
Spg
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
Fsp
|
Spastic Paraplegia, Familial
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
Paraplegia |
Paraplegia, Lower
|
Severe Or Complete Loss Of Motor Function In The Lower Extremities And Lower Portions Of The Trunk
|
|
|
Demyelinating Disease |
Demyelinating Diseases
|
Demyelinating Disorder
|
|
|
Primary Progressive Multiple Sclerosis |
Ppms
|
Primary-Progressive Ms
|
Multiple Sclerosis, Primary Progressive
|
|
|
Optic Neuritis |
Inflammatory Optic Neuropathy
|
|
|
Leukodystrophy |
|
|
Spasticity |
|
|
Spastic Quadriplegia |
Spastic Quadriplegic Cerebral Palsy
|
Quadriplegic Infantile Cerebral Palsy
|
Tetraplegic Infantile Cerebral Palsy
|
Cerebral Palsy Spastic Quadriplegic
|
Quadriplegic Cerebral Palsy
|
Spastic Quadriplegia Cerebral Palsy
|
Spastic Tetraplegia Cerebral Palsy
|
Cerebral Palsy, Quadriplegic, Infantile
|
Cerebral Palsy With Spastic Tetraplegia
|
Congenital Spastic Quadriplegia
|
Spastic Tetraplegic Cerebral Palsy
|
Congenital Quadriplegia Nos
|
Tetraplegic Cerebral Palsy
|
|
|
Striatonigral Degeneration |
|
|
Pelizaeus-Merzbacher-Like Disease |
|
|
Quadriplegia |
|
|
Metachromatic Leukodystrophy |
Arylsulfatase A Deficiency
|
MLD
|
Arsa Deficiency
|
Sulfatide Lipidosis
|
Metachromatic Leukoencephalopathy
|
Cerebral Sclerosis, Diffuse, Metachromatic Form
|
Cerebroside Sulfatase Deficiency
|
Leukodystrophy, Metachromatic
|
Pseudoarylsulfatase A Deficiency
|
Leukodystrophy Metachromatic
|
Sulfatidosis
|
Metachromatic Leukodystrophy, Late Infantile
|
Metachromatic Leukodystrophy Variant
|
Deficiency Of Cerebroside-Sulfatase
|
Scholz Cerebral Sclerosis
|
Sulfatide Lipoidosis
|
Cerebral Sclerosis Diffuse Metachromatic Form
|
Arylsulfatase A Deficiency Disease
|
Cerebroside Sulphatase Deficiency Disease
|
Greenfield Disease
|
Metachromatic Leukodystrophy, Adult
|
Metachromatic Leukodystrophy, Juvenile
|
Leukodystrophy Metachromatic Adult
|
Leukodystrophy Metachromatic Juvenile
|
Leukodystrophy Metachromatic Late Infantile
|
Metachromatic Leukodystrophy, Adult Type
|
Metachromatic Leukodystrophy, Juvenile Type
|
Metachromatic Leukodystrophy, Infant
|
Greenfield'S Disease
|
|
|
Multiple Sclerosis |
MS
|
Multiple Sclerosis, Susceptibility To
|
Disseminated Sclerosis
|
Multiple Sclerosis, Disease Progression, Modifier Of
|
Insular Sclerosis
|
Multiple Sclerosis Modifier Of Disease Progression
|
Multiple Sclerosis, Susceptibility To 1
|
Multiple Sclerosis, Susceptibility To, 1
|
Multiple Sclerosis 1
|
Generalized Multiple Sclerosis
|
Multiple Sclerosis Variant
|
Multiple Sclerosis Susceptibility To
|
Cerebrospinal Sclerosis
|
Generalised Multiple Sclerosis
|
Ms - [Multiple Sclerosis]
|
Disseminated Cerebrospinal Sclerosis
|
Disseminated Multiple Sclerosis
|
Disseminated Nervous System Myelosclerosis
|
Multiple Cerebrospinal Sclerosis
|
Multiple Combined Sclerosis
|
Multiple Sclerosis Generalised
|
Disseminated Brain Sclerosis
|
Disseminated Spinal Sclerosis
|
Insular Brain Sclerosis
|
Miliary Brain Sclerosis
|
Multiple Combined Sclerosis Of Spinal Cord
|
Multiple Ascending Sclerosis
|
Multiple Brain Sclerosis
|
Multiple Sclerosis Of Brain Stem
|
Multiple Sclerosis Of The Brain Stem
|
Multiple Sclerosis Of Cord
|
Sclérose En Plaques
|
Plaque Sclerosis
|
Multiple Sclerosis Of The Spinal Cord
|
|
|
Myasthenia Gravis |
MG
|
Acquired Myasthenia
|
Autoimmune Myasthenia Gravis
|
Erb-Goldflam Disease
|
Mg - [Myasthenia Gravis]
|
Myasthenia Gravis Nos
|
Myasthenia
|
|
|
Spastic Paraplegia 44, Autosomal Recessive |
SPG44
|
Hereditary Spastic Paraplegia 44
|
Autosomal Recessive Spastic Paraplegia 44
|
Autosomal Recessive Spastic Paraplegia Type 44
|
Paraplegia, Spastic, Type 44, Autosomal Recessive
|
|
|
Cerebral Degeneration |
Brain Degeneration
|
Degenerative Brain Disorder
|
|
|
Hypomyelinating Leukoencephalopathy |
|
|
Leukodystrophy, Hypomyelinating, 2 |
Pmld1
|
Hypomyelinating Leukodystrophy 2
|
HLD2
|
Pelizaeus-Merzbacher-Like Disease 1
|
Pelizaeus-Merzbacher-Like Disease Due To Gjc2 Mutation
|
Pelizaeus-Merzbacher-Like Disease Type 1
|
Pelizaeus-Merzbacher-Like Disease, 1
|
Pelizaeus Merzbacher Like Disease
|
Pelizaeus-Merzbacher-Like Disease
|
Pmld - Pelizaeus Merzbacher Like Disease
|
Pelizaeus-Merzbacher-Like Disease Autosomal Recessive Type 1
|
Pmldar1
|
Leukodystrophy, Hypomyelinating, Type 2
|
|
|
Cocaine Abuse |
Cocaine-Related Disorders
|
|
|
Niemann-Pick Disease, Type A |
Niemann-Pick Disease Type A
|
Sphingomyelin Lipidosis
|
Sphingomyelinase Deficiency
|
Niemann-Pick Disease, Intermediate, Protracted Neurovisceral
|
Acid Sphingomyelinase Deficiency, Neurovisceral Type
|
Asmd, Neurovisceral Type
|
Infantile Neurovisceral Acid Sphingomyelinase Deficiency
|
Infantile Neurovisceral Asmd
|
Npd-A
|
Niemann-Pick Disease A
|
NPDA
|
Classical Niemann-Pick Disease
|
Niemann-Pick Disease Acute Neuronopathic Form
|
Niemann-Pick Disease Acute Neurovisceral Form
|
Niemann-Pick Disease Classical Infantile Form
|
Niemann-Pick Disease Intermediate Protracted Neurovisceral
|
Niemann-Pick Disease Neuronopathic Type
|
Niemann-Pick Disease Type I
|
Npa
|
Niemann-Pick Diseases
|
|
|
Leukodystrophy, Hypomyelinating, 7, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism |
HLD7
|
Leukoencephalopathy-Ataxia-Hypodontia-Hypomyelination Syndrome
|
Addh
|
Leukodystrophy, Hypomyelinating, With Hypodontia And Hypogonadotropic Hypogonadism
|
4h Syndrome
|
4h Leukodystrophy 1
|
Hypomyelinating Leukodystrophy 7 With Or Without Oligodontia And-Or Hypogonadotropic Hypogonadism
|
Hypomyelination-Cerebellar Atrophy-Hypoplasia Of The Corpus Callosum Syndrome
|
Leukodystrophy With Oligodontia
|
Tach Syndrome
|
Tremor-Ataxia-Central Hypomyelination Syndrome
|
Leukoencephalopathy, Hypomyelinating, With Ataxia And Delayed Dentition
|
Ataxia, Delayed Dentition, And Hypomyelination
|
Ataxia-Delayed Dentition-Hypomyelination Syndrome
|
Odontoleukodystrophy
|
Dentoleukoencephalopathy
|
Hypomyelinating Leukodystrophy-Ataxia-Hypodontia-Hypomyelination Syndrome
|
Ataxia-Delayed Dentition-Hypomyelination Syndrome
|
Ataxia Delayed Dentition And Hypomyelination
|
Leukodystrophy Hypomyelinating With Hypodontia And Hypogonadotropic Hypogonadism 4h Syndrome
|
Leukoencephalopathy Hypomyelinating With Ataxia And Delayed Dentition
|
Tach
|
Tremor-Ataxia With Central Hypomyelination
|
Attention Deficit Hyperactivity Disorder
|
Leukodystrophy, Dysmyelinating, With Oligodontia
|
|
|
Spastic Paraplegia 75, Autosomal Recessive |
SPG75
|
Hereditary Spastic Paraplegia 75
|
Autosomal Recessive Spastic Paraplegia Type 75
|
Autosomal Recessive Spastic Paraplegia 75
|
|
|
Cerebral Palsy |
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
Palsy Cerebral
|
Palsy, Cerebral
|
Cerebral Palsy, Mixed
|
|
|
Autoimmune Disease |
Autoimmune Diseases
|
Autoimmune Hypersensitivity Disease
|
Hypersensitivity Reaction Type Ii Disease
|
Type Ii Hypersensitivity Reaction Disease
|
|
|
Charcot-Marie-Tooth Disease |
Cmt
|
Hmsn
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
Niemann-Pick Disease |
Sphingomyelin/Cholesterol Lipidosis
|
Niemann-Pick Diseases
|
Lipoid Histiocytosis
|
Sphingomyelin Lipidosis
|
Sphingomyelinase Deficiency Disease
|
Lipid Histiocytosis
|
Neuronal Cholesterol Lipidosis
|
Neuronal Lipidosis
|
Npd
|
Sphingomyelinase Deficiency
|
Niemann-Pick Disease, Type A
|
|
|
Central Nervous System Disease |
Cns Disorder
|
CNS
|
Cns Diseases
|
Central Nervous System Diseases
|
|
|
Charcot-Marie-Tooth Disease And Deafness |
Charcot-Marie-Tooth Disease Type 1e
|
CMT1E
|
Charcot-Marie-Tooth Disease Type 1
|
Hereditary Motor And Sensory Neuropathy Type 1
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
|
Charcot-Marie-Tooth Disease, Type I
|
Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant
|
Charcot-Marie-Tooth Disease, Type 1e
|
Charcot-Marie-Tooth Disease Demyelinating Type 1e
|
Autosomal Dominant Demyelinating Charcot-Marie-Tooth Disease
|
Cmt1
|
Charcot-Marie-Tooth Neuropathy Type 1
|
Autosomal Dominant Charcot-Marie-Tooth Neuropathy And Deafness
|
Charcot-Marie-Tooth Disease-Deafness
|
Charcot-Marie-Tooth Type 1
|
Hmsn1
|
Hereditary Motor And Sensory Neuropathy 1
|
Cmt 1e
|
Charcot Marie Tooth Disease Type 1e
|
Charcot-Marie-Tooth Disease-Deafness Syndrome
|
Charcot-Marie-Tooth Disease-Hearing Loss Syndrome
|
Charcot-Marie-Tooth Disease 1e
|
Charcot-Marie-Tooth Disease And Deafness Autosomal Dominant
|
Charcot-Marie-Tooth Neuropathy Type 1e
|
Charcot-Marie-Tooth Disease, Type Ie
|
Hereditary Motor And Sensory Neuropathy Type I
|
|
|
Leukodystrophy, Hypomyelinating, 4 |
Mitochondrial Hsp60 Chaperonopathy
|
Hypomyelinating Leukodystrophy 4
|
HLD4
|
Mitchap60 Disease
|
Pelizaeus-Merzbacher-Like Disease Due To Hspd1 Mutation
|
Mitchap-60 Disease
|
Leukodystrophy, Hypomyelinating, Type 4
|
|
|
Hypomyelinating Leukodystrophy |
Hld
|
Leukodystrophy, Hypomyelinating
|
|
|
Megalencephalic Leukoencephalopathy With Subcortical Cysts |
Vacuolating Megalencephalic Leukoencephalopathy With Subcortical Cysts
|
Mlc
|
Van Der Knaap Disease
|
Lvm
|
Leukoencephalopathy With Swelling And Cysts
|
Megalencephaly-Cystic Leukodystrophy
|
Megalencephalic Leukodystrophy Megalencephaly-Cystic Leukodystorphy Syndrome
|
Infantile Leukoencephalopathy And Megalencephaly
|
Leukoencephalopathy With Swelling And A Discrepantly Mild Course
|
Vacuolating Leukoencephalopathy
|
Megalencephalic Leukodystrophy
|
Megalencephaly-Cystic Leukodystrophy Syndrome
|
Van Der Knaap Syndrome
|
Leukoencephalopathy, Megalencephalic, With Subcortical Cysts
|
|
|
Spastic Cerebral Palsy |
Palsy, Cerebral, Spastic
|
Infantile Hemiplegia Nos
|
Postnatal Infantile Hemiplegia Nos
|
Congenital Spastic Hemiplegia
|
Spastic Hemiplegic Cerebral Palsy
|
Congenital Hemiplegia Nos
|
Hemiplegic Cerebral Palsy
|
Hemiplegic Infantile Cerebral Palsy
|
|
|
Canavan Disease |
Aspartoacylase Deficiency
|
Aminoacylase 2 Deficiency
|
Spongy Degeneration Of Central Nervous System
|
Aspa Deficiency
|
Acy2 Deficiency
|
Canavan-Van Bogaert-Bertrand Disease
|
Mild Canavan Disease
|
Asp Deficiency
|
Spongy Degeneration Of The Central Nervous System
|
Severe Canavan Disease
|
Von Bogaert-Bertrand Disease
|
Canavan'S Disease
|
Spongy Degeneration Of The Brain
|
Juvenile Canavan Disease
|
Infantile Canavan Disease
|
Neonatal Canavan Disease
|
CAND
|
Disease, Canavan
|
Canavan Disease, Juvenile
|
Canavan Disease, Infantile
|
Canavan Disease, Neonatal
|
|
|
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant |
ADLD
|
Adult-Onset Autosomal Dominant Demyelinating Leukodystrophy
|
Leukodystrophy, Adult-Onset, Autosomal Dominant
|
Adult-Onset Autosomal Dominant Leukodystrophy
|
Autosomal Dominant Leukodystrophy With Autonomic Disease
|
Autosomal Dominant Adult-Onset Demyelinating Leukodystrophy
|
Multiple Sclerosis-Like Disorder
|
Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type, Formerly
|
Autosomal-Dominant Or Late-Onset Type Pelizaeus-Merzbacher Disease
|
Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type
|
Adult-Onset Autosomal Dominant Leukodystrophy With Autonomic Symptoms
|
Lmnb1-Related Adult-Onset Autosomal Dominant Leukodystrophy
|
Leukodystrophy, Demyelinating, Autosomal Dominant, Adult-Onset
|
Pelizaeus-Merzbacher Disease Autosomal Dominant
|
Pelizaeus-Merzbacher Disease Late-Onset Type
|
Adult Onset Autosomal Dominant Leukodystrophy
|
|
|
Hereditary Neuropathies |
|
|
Gene Duplication Disease |
Gene Duplication Syndrome
|
|
|
Alexander Disease |
Alexander'S Disease
|
ALXDRD
|
Alexanders Leukodystrophy
|
Axd
|
Demyelinogenic Leukodystrophy
|
Megalencephaly In Infancy Accompanied By Progressive Spasticity And Dementia
|
Alx
|
Dysmyelinogenic Leukodystrophy
|
Fibrinoid Degeneration Of Astrocytes
|
Leukodystrophy With Rosenthal Fibers
|
Alexander Disease Type Ii
|
Axd Type Ii
|
Alexander Disease Type I
|
Axd Type I
|
Alexanders Disease
|
Alexander'S Leukodystrophy
|
|
|
Allan-Herndon-Dudley Syndrome |
AHDS
|
Allan-Herndon Syndrome
|
Monocarboxylate Transporter 8 Deficiency
|
MCT8 DEFICIENCY
|
Mental Retardation, X-Linked, With Hypotonia
|
Triiodothyronine Resistance
|
T3 Resistance
|
Mental Retardation And Muscular Atrophy
|
Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency
|
Intellectual Disability And Muscular Atrophy
|
Monocarboxylate Transporter-8 Deficiency
|
T3 Resisitence
|
Triiodothyronine Resistence
|
X-Linked Intellectual Disability With Hypotonia
|
Mct8 -Specific Thyroid Hormone Cell Transporter Deficiency
|
Monocarboxylate Transporter 8 Deficiency
|
X-Linked Intellectual Disability-Hypotonia Syndrome
|
|
|
Leukodystrophy, Hypomyelinating, 6 |
Habc
|
Hypomyelinating Leukodystrophy 6
|
HLD6
|
H-Abc
|
Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum
|
Leukodystrophy, Hypomyelinating, With Atrophy Of The Basal Ganglia And Cerebellum
|
Hypomyelinating Leukodystrophy With Atrophy Of The Basal Ganglia And Cerebellum
|
HLD
|
Leukodystrophy, Hypomyelinating, Type 6
|
|
|
Krabbe Disease |
Globoid Cell Leukodystrophy
|
Galactosylceramide Beta-Galactosidase Deficiency
|
Galc Deficiency
|
Galactocerebrosidase Deficiency
|
GLD
|
Globoid Cell Leukoencephalopathy
|
Diffuse Globoid Body Sclerosis
|
Gcl
|
Leukodystrophy, Globoid Cell
|
Krabbe'S Leukodystrophy
|
Krabbe Leukodystrophy
|
KRB
|
Beta Galactocerebrosidase Deficiency
|
Krabbe'S Disease
|
Galactosylceramidase Deficiency Disease
|
Galactosylceramide Lipidosis
|
Galactosylcerebrosidase Deficiency
|
Galactosylsphingosine Lipidosis
|
Psychosine Lipidosis
|
Galactosylceramidase Deficiency
|
Infantile Globoid Cell Leukodystrophy
|
Krabbe Brain Sclerosis
|
|
|
Spastic Paraplegia 10, Autosomal Dominant |
SPG10
|
Hereditary Spastic Paraplegia 10
|
Autosomal Dominant Spastic Paraplegia Type 10
|
Spastic Paraplegia 10
|
Spastic Paraplegia 10 With Or Without Peripheral Neuropathy
|
Autosomal Dominant Spastic Paraplegia 10
|
Autosomal Dominant Spastic Paraplegia
|
Spastic Paraplegia, Autosomal Dominant
|
Paraplegia, Spastic, Autosomal Dominant, Type 10
|
|
|
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease |
Pcwh Syndrome
|
PCWH
|
Neurologic Waardenburg-Shah Syndrome
|
Waardenburg-Shah Syndrome, Neurologic Variant
|
Peripheral Demyelinating Neuropathy-Central Dysmyelinating Leukodystrophy-Hirschsprung Disease-Waardenburg Syndrome
|
Peripheral Demyelinating Neuropathy-Central Dysmyelinating Leukodystrophy-Waardenburg Syndrome-Hirschsprung Disease
|
Ws4 Plus
|
Peripheral Demyelinating Neuropathy, Central Dysmyelinating Leukodystrophy, Waardenburg Syndrome And Hirschsprung Disease
|
Waardenburg-Shah Syndrome Neurologic Variant
|
|
|
Cardiomyopathy, Dilated, 1m |
Dilated Cardiomyopathy 1m
|
CMD1M
|
Cardiomyopathy, Dilated 1m
|
Cardiomyopathy, Dilated, Type 1m
|
|
|
Megalencephalic Leukoencephalopathy With Subcortical Cysts 2a |
MLC2A
|
Leukoencephalopathy, Megalencephalic, With Subcortical Cysts, 2a
|
Leukoencephalopathy, Megalencephalic, With Subcortical Cysts, Type 2a
|
|
|
Leukodystrophy, Hypomyelinating, 5 |
Hypomyelination And Congenital Cataract
|
HLD5
|
Hypomyelination-Congenital Cataract Syndrome
|
Hypomyelinating Leukodystrophy 5
|
Hcc
|
Hypomyelination And Congenital Cataract: Hcc
|
Hypomyelination - Congenital Cataract
|
Hypomyelination With Congenital Cataract
|
|
|
Leukoencephalopathy With Vanishing White Matter |
Cree Leukoencephalopathy
|
Vanishing White Matter Disease
|
Ovarioleukodystrophy
|
Vanishing White Matter Leukodystrophy
|
Childhood Ataxia With Central Nervous System Hypomyelinization
|
Cach
|
Cach Syndrome
|
Myelinosis Centralis Diffusa
|
VWM
|
Cle
|
Childhood Ataxia With Central Nervous System Hypomyelination
|
Childhood Ataxia With Diffuse Central Nervous System Hypomyelination
|
Cach/Vwm
|
Cach/Vwm Syndrome
|
Childhood Ataxia With Central Nervous System Hypomyelination/Vanishing White Matter
|
Cree Leukoencehalopathy
|
Late Infantile Cach Syndrome
|
Juvenile Or Adult Cach Syndrome
|
Congenital Or Early Infantile Cach Syndrome
|
Leukodystrophy With Vanishing White Matter
|
|
|
Leukodystrophy, Hypomyelinating, 3 |
Hypomyelinating Leukodystrophy 3
|
HLD3
|
Pelizaeus-Merzbacher-Like Disease Due To Aimp1 Mutation
|
Leukodystrophy, Hypomyelinating 3
|
Perinatal Sudanophilic Leukodystrophy
|
Leukodystrophy, Hypomyelinating, Type 3
|
Pelizaeus-Merzbacher-Like Disease, Autosomal Recessive, 2
|
|
|
Alzheimer'S Disease 1 |
Alzheimer Disease Type 1
|
Alzheimer'S Disease 1, Early Onset
|
|
|
Schizophrenia |
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
Schizophrenia-1
|
Dementia Praecox
|
Schizophrenia 1
|
|
|
Spastic Ataxia |
|
|
Alzheimer Disease, Familial, 1 |
Alzheimer Disease
|
Alzheimer'S Disease
|
Presenile And Senile Dementia
|
AD1
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
Alzheimer Disease 1, Familial
|
AD
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
Alzheimers Dementia
|
Alzheimer Dementia
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
Alzheimer-Type Dementia
|
Dat
|
Primary Senile Degenerative Dementia
|
Sdat
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
Dementia Due To Alzheimer'S Disease
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Alzheimer Disease Type 1
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Alzheimers
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Nervous System Disease |
Abnormality Of The Nervous System
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Nervous System Diseases
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Nervous System Disorder
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